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. 2022 Mar 29;6(20):5659–5667. doi: 10.1182/bloodadvances.2021006131

Table 5.

All-grade AEs reported in >10% of patients and grade 3 to 5 AEs occurring in ≥5% of patients (N = 40)

All-grade AE n (%) Grade 3-5 AE n (%)
Hematologic toxicity Hematologic toxicity
Neutropenia 14 (35.0) Neutropenia 13 (32.5)
Febrile neutropenia 4 (10.0)
Thrombocytopenia 2 (5.0)
Anemia 2 (5.0)
Nonhematologic toxicity Nonhematologic toxicity
Infusion-related reaction 27 (67.5) Lipase increased 12 (30.0)
Cough 23 (57.5) Pneumonia 6 (15.0)
Fatigue 22 (55.0) Colitis 2 (5.0)
Nausea 20 (50.0) Hepatitis 2 (5.0)
Diarrhea 19 (47.5) Hyperglycemia 2 (5.0)
Constipation 17 (42.5) Upper respiratory tract infection 2 (5.0)
Headache 17 (42.5)
Rash 13 (32.5)
Upper respiratory tract infection 13 (32.5)
Lipase increased 12 (30.0)
Pruritus 12 (30.0)
Pyrexia 12 (30.0)
Back pain 10 (25.0)
Chest pain 10 (25.0)
Vomiting 10 (25.0)
Arthralgia 8 (20.0)
Oropharyngeal pain 8 (20.0)
Pneumonia 8 (20.0)
Abdominal pain 7 (17.5)
Dyspepsia 7 (17.5)
Dyspnea 7 (17.5)
Influenza-like illness 7 (17.5)
Nasal congestion 7 (17.5)
Pain in extremity 7 (17.5)
Sinusitis 7 (17.5)
Urinary tract infection 7 (17.5)
Upper abdominal pain 6 (15.0)
Dizziness 6 (15.0)
Hypertension 6 (15.0)
Insomnia 6 (15.0)
Anxiety 5 (12.5)
Decreased appetite 5 (12.5)

AE, adverse event.